Large-scale purification of hepatitis B surface antigen using affinity chromatography

Summary Large-scale purification of hepatitis B surface antigen, applicable to the preparation of potential vaccines for prevention of hepatitis B, is described. The method involves the following steps: precipitation of serum with polyethylene glycol 6000, affinity chromatography on concanavalin A-Sepharose and on -aminononyl-Sepharose, and isopycnic centrifugation.This study was supported by grant 09011 from the National Heart, Lung and Blood Institute. We thank Dr. B. Hollinger for testing HB_sAg samples by a complement fixation test.     

Mammalian spot test with moxnidazole, a 5-nitroimidazole

Moxnidazole [3-(5-nitrol-1-methyl-2-imidazolyl)-methyleneamino-5-morpholinomethyl-2-oxazolidinone, HCl], known to be mutagenic in microbial tests and Drosophila, induced genetic alterations in somatic cells of mice. Ethyl methanesulfonate (EMS) served as positive control.     

Seasonal variations in fat body metabolism of the green frog Rana esculenta (L.).

Rana esculenta (L.), kept under natural conditions, show almost constant body weights in the annual cycle. Fat body weight, however, has a distinct maximum in October decreasing continuously to a May minimum which is also evident in the fat body index. The triglyceride and protein contents show the same course. Suprisingly high amounts of glycogen are found, which reach a maximum in August.     

Effects of thyrotrophic-releasing hormone (TRH) on thermoregulation in the rat

At ambient temperatures (Ta) of both 8 and 22 degrees C, intraventricular administration of TRH (10-80 microgram) produced a dose-dependent hypothermia in rats. The hypothermia was due to both decreased metabolic heat production and cutaneous vasodilatation. In contrast, at 30 degrees C Ta, TRH increased metabolic heat production (due to behavioral excitation) and led to hyperthermia.     

Giant collagen fibres in the gonopodium of the mosquitofishHeteradria formosa,Agassiz, 1853 (Pisces,Poeciliidae)

Summary The gonopodium of the mosquitofishHeteradria formosa was studied by transmission electron microscopy. In cross-section the gonopodium shows the following structure from the outside inwards: mutilayered epidermis, basal lamina and central supporting tissue, in which vessels and nerves are embedded. At the top of the gonopodium giant collagen fibres are found, which measure up to 150 m in length and 6 m in diameter. These fibres reinforce the gonopodium.This research was supported by the Deutsche Forschungsgemeinschaft. Address for reprints: Forschungsgruppe Dermatologie der Universität Heidelberg, Im Neuenheimer Feld 324, D-6900 Heidelberg.     

Circadian rhythm ofβ-glucuronidase

Summary The circadian rhythm of rat liver-glucuronidase has been studied in animals kept under highly standardized laboratory condition. A clear 24 h rhythm has been observed for this enzyme with a peak activity at 01.00 h and a trough at 13.00 h.The work was carried out in Institut für Anatomie I, Medical School, Hannover (Federal Republic of Germany). Supported by grants from Deutsche Forschungsgemeinschaft, Sonderforschungsbereich 146 and VW Stiftung, Hannover A2 11.2000.     

Opposite effects ofβ-adrenoceptor stimulation and 8-bromo-cyclic AMP on potassium efflux in mammalian heart muscle

Summary -adrenoceptor stimulation by isoprenaline increases the potassium efflux in beating guinea-pig atria. This effect is not mimicked by 8-bromo-cyclic AMP, a cyclic AMP analogue which exerts a positive inotropic effect in this preparation.     

The effect ofβ-adrenergic stimulation and blockade on the efflux of PGE1-like material from the isolated perfused rabbit heart

Summary Prostaglandin (PG) release was measured from the isolated perfused rabbit heart. The effects of -adrenergic stimulation and blockade suggest that PG synthesis is regulated in part by adrenergic mechanisms.     

The C-terminal sequence of human and porcine antithrombin III and its homology with human α-1-proteinase inhibitor

Summary The C-terminal amino acid sequences of human and of porcine antithrombin III have been determined as Gly-Arg-Val-Ala-Asn-Pro-Cys-Val-Lys and Gly-Arg-Val-Ala-Asn-Pro-Cys, respectively. These sequences are highly homologous with the C-terminal sequence of human -1-proteinase inhibitor.